Allele Registry

Canonical Allele Identifier: PA104895

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000011032

RCV000852179

RCV003114184

ClinVar Variation:

10319

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Arg2178His	CA255212 NM_000132.4:c.6533G>A